@prefix bfo: <http://purl.obolibrary.org/obo/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_head {
  this: np:hasAssertion dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_assertion ;
    np:hasProvenance dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_provenance ;
    np:hasPublicationInfo dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_assertion a np:Assertion .
  dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_provenance a np:Provenance .
  dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_assertion {
  miriam-gene:672 a ncit:C16612 .
  lld:C1458155 a ncit:C7057 .
  dgn-gda:DGN234b291cf52990a3340f9cf9a4f313e7 sio:SIO_000628 miriam-gene:672 , lld:C1458155 ;
    a sio:SIO_001122 .
}
dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_provenance {
  dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_assertion dcterms:description "[Two variants of nucleotide sequence observed in the number of patients were classified as DNA polymorphisms (P871L and S1436S) rather than mutations as they were not tightly associated with the increased risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:17990525 ;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331 ;
    prov:wasGeneratedBy bfo:ECO_0000203 .
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^xsd:date .
  dgn-void:source_evidence_literature a bfo:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP231079.RAp1eleoN9oCeGhEWEVI35gxAm7lti6laqK-SZ4a6YeaA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:31+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}